In the case of external quality control, the return to conformity of the devices is certified by the compliant results of a second quality control carried out on the device in accordance with the provisions of Article R. 5212-30.
If, after this second inspection, the expected performance of the device is still not achieved, the accredited body shall inform the Director General of the Agence nationale de sécurité du médicament et des produits de santé and the Director General of the regional health agency within whose jurisdiction the operator is established.